This procedure may be used for the determination of α‑Chymotrypsin activity using N-Benzoyl-L-tyrosine ethyl ester (BTEE) as the substrate. It is not to be used to assay α‑Chymotrypsin agarose (Catalog Number C9134). The procedure is a continuous spectrophotometric rate determination (A256, Light path = 1 cm) based on the following reaction:
BTEE – N-Benzoyl-L-tyrosine ethyl ester
Unit Definition – One unit of α‑chymotrypsin will hydrolyze 1.0 µmole of BTEE per minute at pH 7.8 at 25 °C.
Trizma® Base (Product No. T1503)
N‑Benzoyl-L‑Tyrosine Ethyl Ester (Product No. B6125)
Methanol (Product No. M1775)
Calcium chloride, dihydrate (Product No. C3881)
Hydrochloric acid solution (Product No. H9892)
Precautions – Please consult the Safety Data Sheet for information regarding hazards and safe handling practices.
Use ultrapure water (≥18 MΩxcm resistivity at 25 °C) for the preparation of reagents.
Buffer (80 mM Trizma-base Buffer, pH 7.8 at 25 °C) – Prepare a 12.5-fold dilution of stock 1.0 M Trizma Base buffer, prepared using Product No. T1503, with ultrapure water. Adjust the pH to 7.8 at 25 °C using 1 M HCl or 1 M NaOH.
BTEE Solution (1.18 mM N‑Benzoyl-L‑Tyrosine Ethyl Ester) – To prepare 100 mL:
CaCl2 Solution (2 M Calcium Chloride) – Prepare a 294 mg/mL solution using Calcium chloride, dihydrate (Product No. C3881) in ultrapure water.
HCl Solution (1 mM Hydrochloric Acid) – Prepare a 1,000-fold dilution of 1 M Hydrochloric acid solution (Product No. H9892), with ultrapure water in a 100 mL Class A volumetric flask. Cover flask opening and invert several times to ensure complete mixing. Place solution on ice.
Enzyme Solution (α‑Chymotrypsin) – Immediately before use, prepare a solution containing 2‑5 α‑chymotrypsin units/mL in cold (2‑8 °C) HCl Solution.
In a 3.00 mL reaction mix, the final concentrations are 38 mM Tris, 0.55 mM N-Benzoyl-L-Tyrosine Ethyl Ester, 30% (v/v) Methanol, 53 mM Calcium Chloride, 0.03 mM Hydrochloric Acid, and 0.2‑0.5 units of α‑Chymotrypsin.
1. Pipette the following reagents into suitable quartz cuvettes:
2. Mix by inversion and equilibrate to 25 °C using a suitably thermostatted spectrophotometer blanked versus air.
3. Pipette the following reagents into the cuvettes:
4. Immediately mix by inversion and record the increase in A256 for ~5 minutes.
5. Determine the ΔA256/minute for both the blank and test reactions using the maximum linear rate over a one minute interval using at least 4 points.
TV = total volume (mL) of reaction mix in cuvette
df = dilution factor
0.964 = millimolar extinction coefficient of BTEE at 256 nm
VTest = volume (mL) of Enzyme Solution used in assay